GB2146038A - Process for purifying natural gas - Google Patents
Process for purifying natural gas Download PDFInfo
- Publication number
- GB2146038A GB2146038A GB08419401A GB8419401A GB2146038A GB 2146038 A GB2146038 A GB 2146038A GB 08419401 A GB08419401 A GB 08419401A GB 8419401 A GB8419401 A GB 8419401A GB 2146038 A GB2146038 A GB 2146038A
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- United Kingdom
- Prior art keywords
- natural gas
- methanol
- stage
- temperature
- process according
- Prior art date
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title claims description 176
- 239000003345 natural gas Substances 0.000 title claims description 88
- 238000000034 method Methods 0.000 title claims description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 279
- 238000000746 purification Methods 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 229910001868 water Inorganic materials 0.000 claims description 25
- 239000007789 gas Substances 0.000 claims description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 238000000926 separation method Methods 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 12
- 238000010521 absorption reaction Methods 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 5
- 238000011144 upstream manufacturing Methods 0.000 claims description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 24
- 229910002092 carbon dioxide Inorganic materials 0.000 description 12
- 239000001569 carbon dioxide Substances 0.000 description 12
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 11
- 238000002347 injection Methods 0.000 description 11
- 239000007924 injection Substances 0.000 description 11
- 238000001816 cooling Methods 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 239000012528 membrane Substances 0.000 description 6
- 239000007791 liquid phase Substances 0.000 description 5
- 239000002826 coolant Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 3
- 239000007792 gaseous phase Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- -1 but not exclusively Chemical compound 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 229940075799 deep sea Drugs 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000003949 liquefied natural gas Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/0002—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the fluid to be liquefied
- F25J1/0022—Hydrocarbons, e.g. natural gas
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
- B01D53/1406—Multiple stage absorption
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/229—Integrated processes (Diffusion and at least one other process, e.g. adsorption, absorption)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/11—Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0221—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using the cold stored in an external cryogenic component in an open refrigeration loop
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0243—Start-up or control of the process; Details of the apparatus used; Details of the refrigerant compression system used
- F25J1/0257—Construction and layout of liquefaction equipments, e.g. valves, machines
- F25J1/0275—Construction and layout of liquefaction equipments, e.g. valves, machines adapted for special use of the liquefaction unit, e.g. portable or transportable devices
- F25J1/0277—Offshore use, e.g. during shipping
- F25J1/0278—Unit being stationary, e.g. on floating barge or fixed platform
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2205/00—Processes or apparatus using other separation and/or other processing means
- F25J2205/50—Processes or apparatus using other separation and/or other processing means using absorption, i.e. with selective solvents or lean oil, heavier CnHm and including generally a regeneration step for the solvent or lean oil
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2210/00—Processes characterised by the type or other details of the feed stream
- F25J2210/42—Nitrogen
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2220/00—Processes or apparatus involving steps for the removal of impurities
- F25J2220/60—Separating impurities from natural gas, e.g. mercury, cyclic hydrocarbons
- F25J2220/66—Separating acid gases, e.g. CO2, SO2, H2S or RSH
Description
r 1 GB 2 146 038 A 1
SPECIFICATION
Process for purifying natural gas The present invention relates to the purification of natural gas, particularly, but not exclusively, before its transport and/or its liquefaction.
Natural gas, whether in the form of gas combined with crude oil or dry gas, frequently con- tains, on leaving the production field, certain undesirable components such as water, carbon dioxide and hydrogen sulphide, at least a major part of which must be removed before certain operations such as, in particular, transport and/or liq- uefaction of the natural gas.
Numerous processes have already been proposed for purifying natural gas and more particularly for purification with solvents, but these processes require large installations such as ab- sorption columns, which are costly and bulky, and incompatible with deep- sea exploitation or with offshore gas fields or deposits of oil and associated gas, both on account of the technical problems raised by the bulkiness and the exploitation, and of the economic problems.
The future devlopment of the world gas production depends, among other factors, on the development of simpler and less costly processes for purifying the natural gas.
According to the invention there is provided a process for purifying natural gas, comprising injecting methanol into the natural gas, lowering the temperature of the mixture of natural gas and methanol thus produced to a temperature, called the absorption temperature, at which an absorption of undesirable components present in the natural gas by the methanol is produced, and separating the natural gas thus purified from the methanol phase which has absorbed the undesira- ble components, wherein the natural gas to be purified is subjected to a succession of purification stages, in each of which stages methanol is injected into the natural gas, the mixture of natural gas and methanol thus produced is subject to the absorption temperature, and the natural gas is separated from the methanol phase, the partially purified natural gas which leaves a stage other than the last stage enters the stage which follows it, purified natural gas being obtained at the outlet of the last stage, the methanol injected into the natural gas in any stage other than the last stage is the methanol separated at the outiet of the following stage, and at least a part of the methanol separated at the outlet of the first stage is regenerated by removing at least a part of the said undesirable components which it has absorbed and at least a part of the methanol regenerated in this way is injected into the last stage.
A counterflow effect can thus be obtained while in each stage there is a concurrent circulation of the methanol and the natural gas. The quantity of methanol which is employed can be reduced and the plant can be simplified.
Preferably, the temperature of the said separa- tion of the natural gas from the methanol phase in 130 any stage other than the first stage is lower than or equal to the temperature of the said separation in the preceding stage, the temperature of the said separation in the last stage is between -30' and -1000C and the temperature of the said separation in the first stage is below 10'C.
The natural gas to be purified may be subjected to a preliminary purification by permeation, upstream of the first stage of the said succession of purification stages. A preliminary purification by permeation in some cases makes it possible to reduce further the size of the multistage purification plant described above.
The methanol separated at the outlet of the first stage may be regenerated in two successive stages comprising a first stage for separating at least a part of the acid gases and a second stage for separating at least a part of the water. It is then advantageous to carry out an at least partial separation of the water only on a fraction of the total flow of spent methanol and this fraction is, preferably, less than 20%.
In addition, it has been found advantageous to inject methanol containing a weight proportion of water, which is between 5 and 50%, into the natural gas in the last stage.
Another subject of the invention consists in integrating the above described purification process with a process for liquefying natural gas by sup- plying the purified natural gas which leaves the last stage to a final heat exchanger which liquefies the natural gas by means of liquid nitrogen. The natural gas is preferably cooled by a stream of liquid nitrogen which enters the final heat exchanger and which then circulates from one stage to another in the said succession of purification stages in a direction opposite to that of the flow of the natural gas.
Embodiments according to the invention will now be described, by way of example only, with reference to the accompanying drawings.
In the drawings:
Figure 1 shows diagrammatically an embodiment of a plant for purifying natural gas according to the present invention in two successive stages with more extensive cooling in the second stage; Figure 2 shows diagrammatically an embodiment of a plant for regenerating the methanol; Figure 3 shows diagrammatically an embodi- ment of a plant for purifying natural gas with methanol, such as that shown in Figure 1, combined with a plant for purification by gas permeation; Figure 4 shows diagrammatically an embodi- ment of a plant for liquefying natural gas incorporating a plant for purification of natural gas such as that shown in Figure 3:
As shown in Figure 1, natural gas delivered by an inlet pipeline 1 is purified by being placed in contact with methanol, at a low temperature, in two successive purification stages 2 and 3.
Stage 2 incorporates, from upstream to downstream, a methanol injection point 4, a heat exchanger 5 and a separator vessel 6. Methanol is delivered by a methanol entry line 7 to the injec- 2 GB 2 146 038 A 2 tion point 4, so that a mixture of natural gas and methanol flows, downstream of the injection point 4, along an inlet line 8 into the heat exchanger 5. This line 8 is connected to a passage 9 in the heat exchanger. A coolant fluid is delivered to the heat exchanger 5 via a line 10, flows in a passage 11, separate from passage 9, but in thermal contact with the latter, and leaves by a line 12.
During the cooling of the mixture of natural gas and methanol in the passage 9, a part of the undesirable components, such as water and the acid gases carbon dioxide and hydrogen sulphide, is absorbed by the methanol. The mixture of natural gas and methanol leaves the heat exchanger 5 via a line 13 and is delivered to the separator vessel 6 where the liquid and gaseous phases are separated and from which are withdrawn partially purified gas, from the upper part by a fine 14, and spent methanol, from the lower part by a line 15. In some cases and depending on the composition of the natural gas to be purified, a quantity of hydrocarbons can sometimes condense during the cooling in the passage 9, which results in the appearance of a second liquid phase, which is separated in the vessel 6 and removed by a line 16.
Stage 3 incorporates, from upstream to downstream, a methanol injection point 17, a heat exchanger 18 and a separator vessel 19. The line 14 delivers partially purified gas, Methanol is deliv- ered by line 20 to the injection point 17 where methanol is injected so that a mixture of natural gas and methanol flows downstream of the injection point 17 through an inlet line 21 into the heat exchanger 18. Line 21 is connected to a passage 22 in the heat exchanger 18. A coolant fluid is delivered to the heat exchanger 18 via a line 23, flows through a passage 24, separate from passage 22, but in thermal contact with the latter, and leaves by a line 25.
During the cooling of the mixture of natural gas and methanol in the passage 22, a major part of the undesirable components present in the natural gas is absorbed by the methanol. The mixture of natural gas and methanol leaves the heat exchan- ger 18 via a line 26 and is delivered to the separator vessel 19, where the liquid and gaseous phases separate and from which are extracted, purified gas, from the upper part by a line 27, and partially spent methanol, from the lower part by a line 28. If condensation of certain hydrocarbons takes place, a second liquid phase is separated in the vessel 19 and is removed by a line 29.
The partially spent methanol removed by the line 28 is the methanol which is injected into the natu- ral gas circulation at the injection point 4. It is conveyed by a pump 30. At the injection point 17, new methanol is injected. This methanol is essentially, except for the small leaks which must be compensated by an outside supply, the methanol which is at least partially regenerated from the spent methanol leaving via the line 15.
The methanol regeneration plant arranged between the lines 15 and 20 is not shown in Figure 1, because the methanol regeneration plant may be of a conventional type. It may, in particular, incor- porate first a separation of at least a part of the acidic gases, which are light components, by pressure reduction and contact with an inert gas, and then a water separation. Water, being less volatile than methanol, is separated from it, for example by adsorption on a solid or by distillation.
The methanol injected into the line at the injection point 17 via the line 20 may still contain water, preferably in a weight proportion from 5% to 50%.
Its absorbing properties and its freezing point are slightly modified thereby, but remain compatible with its use in the purification process described here. Moreover, in the case where cooling of the natural gas leads to condensation of liquid hydro- carbons, the presence of water in the methanol promotes the separation of these liquid hydrocarbons from the methanol, which reduces the losses of methanol in the said liquid hydrocarbons and the entrainment of hydrocarbons with the metha- no].
It is for this reason that provision may be made for carrying out at least a partial separation of methanol from water in respect of only a fraction of the total flow of recycled methanol, a fraction which is preferably less than 20%. The energy consumption is thus reduced while accumulation of water in the methanol during the operation of the natural gas purification plant is avoided.
Figure 2 shows diagrammatically a methanol re- generation plant with separation of water from methanol carried out only on a branch of the main stream of methanol to be regenerated. The spent methanol leaving on line 15 and carrying various impurities such as water, carbon dioxide and hydrogen sulphide, first passes into a separator 31 for acid gases, in which its pressure is reduced to a pressure below that of the treated natural gas, and, if appropriate, is contacted with an inert carried gas. At least a part of the carbon dioxide and of the hydrogen sulphide is separated from the methanol and leaves the separator 31 via a line 32, while the methanol leaves via a line 33. At a Yjunction 34, the main part of the methanol flowing in the line 33 is directed via a line 35 towards the line 20 for introducing regenerated methanol into stage 3, while a minor proportion of the methanol is lead via a line 36 to a water separator 37 which may be, for example, a distillation column. At least a part of the water is separated from the methanol and leaves via a line 38, the methanol leaving via a line 39 to rejoin the main part of the methanol at a reinjection point 40. The total flow of the regenerated methanol thus obtained circulates in a line 41 under the action of a pump 42, to be reinjected into the natural gas at the injection point 17.
In the embodiment of Figure 1, the natural gas to be purified, mixed with methanol, is cooled in stage 2 to a temperature which is intermediate the temperature in the entry pipeline 1 and the tem- perature in stage 3. For example, the cooling temperature in stage 2 is - 60'C and the cooling temperature in stage 3 is -80'C. it is also possible to carry out a complete cooling in stage 2 merely to maintain stage 3 at the same temperature as that finally attained in stage 2. The final tempera- GB 2 146 038 A 3 3 ture of the natural gas/methanol mixture which is chosen is the lower, the higher the purification which is required in respect of the natural gas.
By splitting up the methanol purification system, into two or more stages, the consumption of methanol is reduced, because the absorption capacity of the latter is utilised better. The methanol consumption is the lower, the greater the number of stages.
The embodiment of Figure 3 is similar to that of Figure 1, except that, upstream of stage 2, a gaseous permeation separator 43 has been introduced, in which a membrane 44 divides an inner space into a supply enclosure 45, through which passes the main stream of natural gas between an inlet pipe 46 delivering the natural gas to be purified and an outlet line 47 connected to the pipe 1, undergoing a small pressure drop, and a permeation enclosure 48 which receives a secondary stream extracted from the total stream of natural gas by permeation through the membrane 44. This secondary stream is rich in componenets such as water, carbon dioxide and hydrogen sulphide. It leaves under a low pressure via a discharge line 49.
The addition of the permeation separator 43 is advantageous where the natural gas incorporates some concentration of undesirable components, because it makes it possible to reduce the rate of methanol circulation and the size of the heat ex- changers 5 and 18. An optimum is to be sought in the purifying role which is assigned, respectively, to the gaseous permeation separator 43 and the methanol mixture absorption system.
The membrane 44 may be a cellulose acetate membrane for acid removal or carbon dioxide purification, at present commercially available. It is also possible advantageously to employ a membrane such as that recommended for use in French Patent Application 83/01,815 of 4th February 1983 for: "Process for gas dehydration" (U.K. Patent Ap- 105 plication No. 8402648).
Figure 4 shows diagrammatically a plant for purifying natural gas which is similar to that of Figure 3, but to which has been added a supplementary plant for liquefying purified gas. An economical unit is thus obtained, with the purified natural gas being already at a low temperature at the outlet of the purification system, before its entry into the liquefying system.
The outlet line 27 for purified natural gas is connected to a passage 50 of a final heat exchanger 51, where the natural gas liquefies and from which it is conveyed by a line 52 to a storage tank 53. The final heat exchanger 51 is cooled by a coolant fluid entering via a line 54, circulating in a passage 55 and leaving via a line 56. This coolantfluid is preferably liquid nitrogen delivered at approximately -195'C.
In the case where liquid nitrogen is employed as coolant in the purification plant it may be advantageous to connect the lines 56 and 23 and the lines 25 and 10, as shown in Figure 4, so that the liquid nitrogen circulates in an opposite direction to that of the natural gas and produces the cooling of all the heat exchangers 51, 18 and 5 in succession.
This implementation is particularly advantageous for working offshore. The plant shown in Figure 4 may be arranged on a platform, on account of its low weight and its small bulk. A tanker can deliver the liquid nitrogen required for opeating the plant and leave with the liquefied natural gas.
The optional devices for liquid hydrocarbon removal have not been shown in this plant, since these devices are of a conventional type.
The process of purification according to Figure 3 may be illustrated with the aid of the following example in which the concentrations are expressed in weight fraction (% or p.p.m.), Natural gas containing 0.089% of water, 0.965% of carbon dioxide and 7.45% of hydrogen sulphide is supplied to delivery line 46 at a pressure of 4.2 x 106 Pa and a temperature of 2WC, at a weight flow rate of 36 tonnes/hour. The part of this natural gas, which after having passed through the membrane 44 of separator 43 leaves by the discharge line 49, contains 0.83% of water, 4. 95% of carbon dioxide and 54.3% of hydrogen sulphide. It is at a temperature of 2WC and a pressure of 0.15 x 106 Pa and its flow rate is 3 tonnes/hour. The main stream of natural gas leaving at line 47 from the gaseous permeation separator 43 contains 0.0147% of water, 0.74% of carbon dioxide and 2.541/6 of hydrogen sulphide. Its temperature is 2WC, its pressure is 4 x 101; Pa and its weight flowrate is 33 tonnes/hour.
At the injection point 4, the natural gas stream receives via the line 7 methanol containing 1.5 p.p.m. of water, 89 p.p.m. of carbon dioxide and 46 p.p.m. of hydrogen sulphide. After being cooled to -WC in the heat exchanger 5, the liquid phase leaving via the line 15 contains 16 p.p.m. of water, 0.082% of carbon dioxide and 0.28% of hydrogen sulphide.
The gaseous phase leaving via the line 14 receives at the injection point 20 a flow of 300 tonnes/hour of new and/or regenerated methanol. After cooling to -WC in the heat exchanger 18, there is obtained in line 27 a purified natural gas which now only contains 0,6 p.p.m. of water, 50 p.p.m. of carbon dioxide and 2.8 p.p.m. of hydrogen sulphide.
Naturally, this example is given by way of illustration only of one of the possible embodiments of the process according to the invention. Numerous alternative forms and modifications can, moreover, be introduced into the systems shown in the draw ings, without departing from the scope of the invention.
There is thus provided a simple process for puri- fying natural gas, which is capable of being integrated particularly into a liquefaction process and capable, if appropriate, of being employed on an offshore platform. Additionally, the consumption of solvent in a particular solvent-type process for pu- rifying natural gas can be reduced.
Claims (12)
1. Process for purifying natural gas, comprising injecting methanol into the natural gas, lowering 4 GB 2 146 038 A 4 the temperature of the mixture of natural gas and methanol thus produced to a temperature, called the absorption temperature, at which an absorption of undesirable components present in the natural gas by the methanol is produced, and separating the natural gas thus purified from the methanol phase which has absorbed the undesirable components, wherein the natural gas to be purified is subjected to a succession of purification stages, in each of which stages methanol is injected into the natural gas, the mixture of natural gas and methanol thus produced is subject to the absorption temperature, and the natural gas is separated from the methanol phase, the partially puri- fied natural gas which leaves a stage other than the last stage enters the stage which follows it, purified natural gas being obtained at the outlet of the last stage, the methanol injected into the natural gas in any stage other than the last stage is the methanol separated at the outlet of the following stage, and at least a part of the methanol separated at the outlet of the first stage is regenerated by removing at least a part of the said undesirable components which it has absorbed and at least a part of the methanol regenerated in this way is injected into the last stage.
2. A process according to claim 1, wherein the natural gas to be purified is subjected to a preliminary purification by permeation upstream of the first stage of the said succession of purification stages.
3. A process according to either claim 1 or claim 2, wherein the temperature of the said separation of natural gas from the methanol phase, in any stage other than the first stage, is lower than or equal to the temperature of the said separation of the natural gas from the methanol phase from the preceding stage.
4. A process according to claim 3, wherein the temperature of the said separation of the natural gas from the methanol phase from the last stage is between -30T and -100T.
5. A process according to one of the preceding claims, wherein the temperature of the said sepa- ration of the natural gas from the methanol phase from the first stage is below 100C.
6. A process according to any one of the preceding claims, wherein the methanol separated at the outlet of the first stage is regenerated in two successive steps comprising a first step for separating at least a part of the acid gases and a second step for separating water, and the separation of at least a part of the water is carried out only on a fraction of the total flow of methanol.
7. A process according to claim 6, wherein the said fraction of the total flow of methanol is below 20%.
8. A process according to any one of the preceding claims, wherein methanol containing a weight proportion of water of between 5 and 50% is injected into the natural gas in the last stage.
9. A process according to one of the preceding claims, associated with a liquefaction process, wherein the purified natural gas obtained in the last stage of the purification process is supplied to a final heat exchanger causing the liquefaction of the natural gas by means of liquid nitrogen.
10. A process according to claim 9, wherein a stream of liquid nitrogen is introduced into the said final heat exchanger and circulates from one stage to another of the said succession of purification stages in a direction opposite to the direction of flow of the natural gas.
11. A process for purifying natural gas substan- tially as herein described with reference to the accompanying drawings.
12. A process for purifying and liquefying natural gas substantially as herein described with reference to the accompanying drawings.
Printed in the UK for HMSO, D881C935, 2,85, 7102. Published by The Patent Office, 25 Southampton Buildings, London, WC2A lAY, from which copies may be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8313767A FR2550956B1 (en) | 1983-08-26 | 1983-08-26 | PROCESS FOR THE PURIFICATION OF A NATURAL GAS, WHICH MAY IN PARTICULAR BE INTEGRATED INTO A PROCESS FOR LIQUEFACTION OF THIS NATURAL GAS |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8419401D0 GB8419401D0 (en) | 1984-09-05 |
GB2146038A true GB2146038A (en) | 1985-04-11 |
GB2146038B GB2146038B (en) | 1987-04-01 |
Family
ID=9291826
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08419401A Expired GB2146038B (en) | 1983-08-26 | 1984-07-30 | Process for purifying natural gas |
Country Status (4)
Country | Link |
---|---|
US (1) | US4606741A (en) |
FR (1) | FR2550956B1 (en) |
GB (1) | GB2146038B (en) |
NO (1) | NO163317C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2326423A (en) * | 1997-06-17 | 1998-12-23 | Inst Francais Du Petrole | Process for degasolining a gas containing condensable hydrocarbons |
Families Citing this family (26)
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FR2605241B1 (en) * | 1986-10-16 | 1989-10-27 | Inst Francais Du Petrole | INTEGRATED PROCESS FOR TREATING METHANE-CONTAINING WET GAS FOR THE PURPOSE OF REMOVING WATER |
FR2636857B1 (en) * | 1988-09-26 | 1990-12-14 | Inst Francais Du Petrole | PROCESS FOR DEHYDRATION, DEACIDIFICATION AND SEPARATION OF CONDENSATE FROM NATURAL GAS |
AT394953B (en) * | 1990-07-23 | 1992-08-10 | Schmid Peter J | Process for removing hydrogen sulphide from gas mixtures |
FR2733162B1 (en) * | 1995-04-19 | 1997-06-06 | Inst Francais Du Petrole | METHOD AND DEVICE FOR REMOVING AT LEAST ONE SOLVENT-ACID GAS FOR THE PURIFICATION OF NATURAL GAS |
FR2739789B1 (en) * | 1995-10-11 | 1997-11-21 | Inst Francais Du Petrole | METHOD AND DEVICE FOR TREATING A GAS CONTAINING WATER SUCH AS A NATURAL GAS |
FR2743083B1 (en) * | 1995-12-28 | 1998-01-30 | Inst Francais Du Petrole | METHOD FOR DEHYDRATION, DEACIDIFICATION AND DEGAZOLINATION OF A NATURAL GAS, USING A MIXTURE OF SOLVENTS |
DE19622692C1 (en) * | 1996-06-05 | 1998-01-15 | Linde Ag | Liquefaction of hydrocarbon-rich gas stream containing aromatic and heavy hydrocarbon(s) |
FR2757423B1 (en) * | 1996-12-19 | 1999-01-29 | Inst Francais Du Petrole | METHOD AND DEVICE FOR TREATING A GAS BY REFRIGERATION AND CONTACT WITH A SOLVENT |
NL1006013C2 (en) * | 1997-05-09 | 1998-11-10 | Tno | Apparatus and method for performing membrane gas / liquid absorption at elevated pressure. |
US6168768B1 (en) * | 1998-01-23 | 2001-01-02 | Exxon Research And Engineering Company | Production of low sulfer syngas from natural gas with C4+/C5+ hydrocarbon recovery |
FR2822839B1 (en) * | 2001-03-29 | 2003-05-16 | Inst Francais Du Petrole | IMPROVED PROCESS FOR DEHYDRATION AND DEGAZOLINATION OF A WET NATURAL GAS |
DE10338563A1 (en) * | 2003-08-22 | 2005-03-17 | Basf Ag | Removing acid gases from fluid stream, especially natural gas, comprises using membrane unit comprising porous membrane in housing with plastic or rubber interior surface |
US8293186B2 (en) * | 2004-07-29 | 2012-10-23 | Gas Technologies Llc | Method and apparatus for producing methanol |
US7642293B2 (en) * | 2004-07-29 | 2010-01-05 | Gas Technologies Llc | Method and apparatus for producing methanol with hydrocarbon recycling |
US7578981B2 (en) * | 2004-07-29 | 2009-08-25 | Gas Technologies Llc | System for direct-oxygenation of alkane gases |
US7910787B2 (en) * | 2004-07-29 | 2011-03-22 | Gas Technologies Llc | Method and system for methanol production |
US9180426B2 (en) * | 2004-07-29 | 2015-11-10 | Gas Technologies, Llc | Scrubber for methanol production system |
US8202916B2 (en) * | 2004-07-29 | 2012-06-19 | Gas Technologies Llc | Method of and apparatus for producing methanol |
US7456327B2 (en) | 2004-07-29 | 2008-11-25 | Gas Technologies, Llc | Method for direct-oxygenation of alkane gases |
US7879296B2 (en) * | 2005-12-27 | 2011-02-01 | Gas Technologies Llc | Tandem reactor system having an injectively-mixed backmixing reaction chamber, tubular-reactor, and axially movable interface |
US7687669B2 (en) | 2005-12-27 | 2010-03-30 | Gas Technologies Llc | Method for direct-oxygenation of alkane gases |
DE102006045031A1 (en) * | 2006-09-23 | 2008-03-27 | Linde Ag | Method for providing natural gas |
US20120247327A1 (en) * | 2010-09-27 | 2012-10-04 | Conocophillips Company | Hollow-fiber membrane contactors |
WO2013136310A1 (en) * | 2012-03-16 | 2013-09-19 | Aker Process Systems As | Hydrocarbon gas treatment |
US11493270B2 (en) | 2019-05-24 | 2022-11-08 | Praxair Technology, Inc. | Dual mode Liquefied Natural Gas (LNG) liquefier |
CN115701449A (en) * | 2021-08-02 | 2023-02-10 | 中国石油天然气股份有限公司 | Liquefied petroleum gas production system meeting copper sheet corrosion requirements |
Citations (1)
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GB1196658A (en) * | 1966-10-14 | 1970-07-01 | Metallgesellschaft Ag | A Process for Removing Hydrogen Sulphide and Carbon Dioxide from Fuel Gases and Synthesis Gases Containing the Same |
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FR1051410A (en) * | 1950-12-09 | 1954-01-15 | Lindes Eismaschinen Ag | Process for drying and purifying natural gas or cracking or hydrogenation exhaust gas |
US3416324A (en) * | 1967-06-12 | 1968-12-17 | Judson S. Swearingen | Liquefaction of a gaseous mixture employing work expanded gaseous mixture as refrigerant |
US3899312A (en) * | 1969-08-21 | 1975-08-12 | Linde Ag | Extraction of odorizing sulfur compounds from natural gas and reodorization therewith |
US3886757A (en) * | 1970-12-24 | 1975-06-03 | Phillips Petroleum Co | Reduction of hydrate formation in a natural gas stream by contacting with anit-freeze agent |
US3977203A (en) * | 1974-03-25 | 1976-08-31 | Kansas University Endowment Association | Purification of natural gas by liquid/liquid extraction with a polar solvent |
US4130403A (en) * | 1977-08-03 | 1978-12-19 | Cooley T E | Removal of H2 S and/or CO2 from a light hydrocarbon stream by use of gas permeable membrane |
US4475347A (en) * | 1982-09-16 | 1984-10-09 | Air Products And Chemicals, Inc. | Process for separating carbon dioxide and sulfur-containing gases from a synthetic fuel production process off-gas |
-
1983
- 1983-08-26 FR FR8313767A patent/FR2550956B1/en not_active Expired
-
1984
- 1984-07-30 GB GB08419401A patent/GB2146038B/en not_active Expired
- 1984-08-24 NO NO843389A patent/NO163317C/en unknown
-
1985
- 1985-08-09 US US06/763,896 patent/US4606741A/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1196658A (en) * | 1966-10-14 | 1970-07-01 | Metallgesellschaft Ag | A Process for Removing Hydrogen Sulphide and Carbon Dioxide from Fuel Gases and Synthesis Gases Containing the Same |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2326423A (en) * | 1997-06-17 | 1998-12-23 | Inst Francais Du Petrole | Process for degasolining a gas containing condensable hydrocarbons |
GB2326423B (en) * | 1997-06-17 | 2002-01-23 | Inst Francais Du Petrole | Process for degasolining a gas containing condensable hydrocarons |
Also Published As
Publication number | Publication date |
---|---|
GB2146038B (en) | 1987-04-01 |
FR2550956B1 (en) | 1985-10-25 |
US4606741A (en) | 1986-08-19 |
NO163317B (en) | 1990-01-29 |
FR2550956A1 (en) | 1985-03-01 |
NO163317C (en) | 1990-05-09 |
GB8419401D0 (en) | 1984-09-05 |
NO843389L (en) | 1985-02-27 |
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Legal Events
Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19940730 |